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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EEF2, LOC130063169
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
EEF2
Single nucleotide variant
(synonymous variant)
Spinocerebellar ataxia type 26
+1 more
GBenign
EEF2
(P390L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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